AU2014223496B2 - Glyphosate composition for dicamba tank mixtures with improved volatility - Google Patents
Glyphosate composition for dicamba tank mixtures with improved volatility Download PDFInfo
- Publication number
- AU2014223496B2 AU2014223496B2 AU2014223496A AU2014223496A AU2014223496B2 AU 2014223496 B2 AU2014223496 B2 AU 2014223496B2 AU 2014223496 A AU2014223496 A AU 2014223496A AU 2014223496 A AU2014223496 A AU 2014223496A AU 2014223496 B2 AU2014223496 B2 AU 2014223496B2
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- AU
- Australia
- Prior art keywords
- glyphosate
- carbon atoms
- salt
- hydrocarbyl
- dicamba
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 267
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims abstract description 239
- 239000005562 Glyphosate Substances 0.000 title claims abstract description 183
- 229940097068 glyphosate Drugs 0.000 title claims abstract description 183
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 title claims abstract description 119
- 239000005504 Dicamba Substances 0.000 title claims abstract description 96
- 239000012141 concentrate Substances 0.000 claims abstract description 125
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- 238000000034 method Methods 0.000 claims abstract description 37
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- 239000012895 dilution Chemical class 0.000 claims abstract description 20
- 238000010790 dilution Methods 0.000 claims abstract description 20
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims abstract description 13
- 238000011068 loading method Methods 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 104
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- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 50
- 125000000217 alkyl group Chemical group 0.000 claims description 39
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- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 230000008238 biochemical pathway Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
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- 210000002421 cell wall Anatomy 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002304 glucoses Chemical class 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical class NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 125000002951 idosyl group Chemical class C1([C@@H](O)[C@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- NPFOYSMITVOQOS-UHFFFAOYSA-K iron(III) citrate Chemical compound [Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NPFOYSMITVOQOS-UHFFFAOYSA-K 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
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- 239000011707 mineral Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
- BXYVQNNEFZOBOZ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-n',n'-dimethylpropane-1,3-diamine Chemical compound CN(C)CCCNCCCN(C)C BXYVQNNEFZOBOZ-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
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- 239000008117 stearic acid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
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- 230000009261 transgenic effect Effects 0.000 description 1
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- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Toxicology (AREA)
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US61/769,943 | 2013-02-27 | ||
PCT/US2014/018829 WO2014134235A1 (en) | 2013-02-27 | 2014-02-27 | Glyphosate composition for dicamba tank mixtures with improved volatility |
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AU2014223496A1 AU2014223496A1 (en) | 2015-09-03 |
AU2014223496B2 true AU2014223496B2 (en) | 2017-11-30 |
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AU2014223496A Active AU2014223496B2 (en) | 2013-02-27 | 2014-02-27 | Glyphosate composition for dicamba tank mixtures with improved volatility |
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EP (1) | EP2961276B1 (es) |
CN (2) | CN105072912A (es) |
AR (2) | AR094909A1 (es) |
AU (1) | AU2014223496B2 (es) |
BR (1) | BR112015020639B1 (es) |
CA (3) | CA2901680C (es) |
DK (1) | DK2961276T3 (es) |
ES (1) | ES2694509T3 (es) |
HK (1) | HK1219621A1 (es) |
HU (1) | HUE040466T2 (es) |
MX (1) | MX2015011054A (es) |
PL (1) | PL2961276T3 (es) |
TR (1) | TR201815726T4 (es) |
UY (1) | UY35352A (es) |
WO (1) | WO2014134235A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
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ATE517548T1 (de) | 2004-03-10 | 2011-08-15 | Monsanto Technology Llc | Herbizide zusammensetzungen, die n- phosphonomethylglycin und ein auxinherbizid enthalten |
ES2317295T3 (es) | 2004-08-19 | 2009-04-16 | Monsanto Technology Llc | Composicion herbicida de sal glifosato. |
US8236731B2 (en) | 2005-05-24 | 2012-08-07 | Monsanto Technology Llc | Herbicide compatibility improvement |
WO2011019652A2 (en) | 2009-08-10 | 2011-02-17 | Monsanto Technology Llc | Low volatility auxin herbicide formulations |
US10334849B2 (en) | 2011-10-26 | 2019-07-02 | Monsanto Technology Llc | Salts of carboxylic acid herbicides |
WO2013184622A2 (en) | 2012-06-04 | 2013-12-12 | Monsanto Technology Llc | Aqueous concentrated herbicidal compositions containing glyphosate salts and dicamba salts |
CA2901680C (en) * | 2013-02-27 | 2021-09-07 | Monsanto Technology Llc | Glyphosate composition for dicamba tank mixtures with improved volatility |
WO2016130813A1 (en) | 2015-02-11 | 2016-08-18 | Adjuvants Plus Usa, Inc. | An agrochemical formulation aid for micronutrient uptake in plants, plant health benefits and herbicide performance |
CN108135160A (zh) * | 2015-07-21 | 2018-06-08 | 瑟拉迪斯有限公司 | 稳定的农用组合物 |
BR112019002613B1 (pt) | 2016-08-09 | 2023-03-07 | Monsanto Technology Llc | Composições sólidas de concentrado de herbicida, seus processos de preparação, e método para preparação de uma mistura aquosa de herbicida |
BR112019026363A2 (pt) * | 2017-06-13 | 2020-07-21 | Monsanto Technology Llc | misturas herbicidas de auxina |
JP7382324B2 (ja) * | 2017-12-22 | 2023-11-16 | モンサント テクノロジー エルエルシー | 除草剤混合物 |
MX2020013209A (es) * | 2018-06-05 | 2021-03-25 | Monsanto Technology Llc | Composiciones herbicidas. |
WO2021113283A1 (en) * | 2019-12-02 | 2021-06-10 | The Board Of Trustees Of The University Of Arkansas | Compositions and methods to reduce dicamba volatility and provide plant essential nutrients |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060270556A1 (en) * | 2005-05-24 | 2006-11-30 | Wright Daniel R | Herbicide compatibility improvement |
US20100113274A1 (en) * | 2008-09-29 | 2010-05-06 | Monsanto Technology Llc | Glyphosate formulations containing amidoalkylamine surfactants |
US20100331182A1 (en) * | 2009-06-25 | 2010-12-30 | Dow Agrosciences Llc | Herbicidal concentrate compositions containing glyphosate and dicamba salts |
Family Cites Families (183)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2505059A (en) | 1946-08-16 | 1950-04-25 | Baker Chem Co J T | 2, 4-d salt and composition containing the same |
GB851008A (en) | 1958-03-28 | 1960-10-12 | Amchem Prod | New amine salts of aromatic acids, their use in herbicidal compositions and processes for their production |
US3013054A (en) | 1958-08-04 | 1961-12-12 | Velsicol Chemical Corp | 2-methoxy-3, 6-dichlorobenzoates |
US3276856A (en) | 1965-03-22 | 1966-10-04 | Amchem Prod | Herbicidal compositions |
US3852340A (en) | 1966-09-26 | 1974-12-03 | Akzona Inc | Plant hormone carboxylic acid salts of aliphatic polyamines |
NL139442B (nl) | 1968-03-21 | 1973-08-15 | Minnesota Mining & Mfg | Werkwijze ter bereiding van een bestrijdingsmiddel. |
US3594151A (en) | 1968-11-12 | 1971-07-20 | Diamond Shamrock Corp | Herbicidally active spray composition |
US3600407A (en) | 1969-04-04 | 1971-08-17 | Velsicol Chemical Corp | Furfuryl-2-methoxy-3,6-dichlorobenzoate |
US3751239A (en) | 1969-05-29 | 1973-08-07 | Rohm & Haas | Herbicidal compositions containing n-(1,1-dialkyl-3-chloroacetonyl) benzamides |
US3799758A (en) | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
US3713404A (en) | 1971-04-16 | 1973-01-30 | Gen Foods Corp | Plant husbandry |
US3870732A (en) | 1973-08-21 | 1975-03-11 | Velsicol Chemical Corp | Mixed salts of aluminum |
US4022610A (en) | 1973-10-15 | 1977-05-10 | Velsicol Chemical Corporation | Herbicidal mixed salts of magnesium |
US3910974A (en) | 1973-10-15 | 1975-10-07 | Velsicol Chemical Corp | Mixed salts of magnesium of 2-methoxy-3,6-dichlorobenzoic acid and a carboxylic acid |
US3923849A (en) | 1973-10-29 | 1975-12-02 | Velsicol Chemical Corp | Aluminum salts of 2-methoxy-3,6-dichlorobenzoic acid |
US4405531A (en) | 1975-11-10 | 1983-09-20 | Monsanto Company | Salts of N-phosphonomethylglycine |
HU182980B (en) | 1979-12-28 | 1984-03-28 | Nitrokemia Ipartelepek | Concentrates and spray solutions containing n-bracket-phosphono-methyl-bracket closed-glycine |
US4936900A (en) | 1983-04-04 | 1990-06-26 | E. I. Du Pont De Nemours And Company | Stabilized aqueous formulations of sulfonylurea salts |
US4692184A (en) | 1984-04-24 | 1987-09-08 | Monsanto Company | 2,6-substituted pyridine compounds |
US4534783A (en) | 1984-01-03 | 1985-08-13 | Monsanto Co. | High concentration encapsulation of water soluble-materials |
US4546196A (en) | 1984-06-11 | 1985-10-08 | Velsicol Chemical Corporation | 3-Chlorobenzyl-3,6-dichloro-2-methoxybenzoate |
CA1242748A (en) | 1984-11-26 | 1988-10-04 | Rita S. Jones | Salt of dicamba |
USH224H (en) | 1985-05-30 | 1987-03-03 | A. E. Staley Manufacturing Company | Glycoside-containing agricultural treatment composition |
US5188958A (en) | 1986-05-29 | 1993-02-23 | Calgene, Inc. | Transformation and foreign gene expression in brassica species |
US4936901A (en) | 1986-07-09 | 1990-06-26 | Monsanto Company | Formulations of water-dispersible granules and process for preparation thereof |
US4729781A (en) | 1986-08-04 | 1988-03-08 | Sandoz Ltd. | 3,6-dichloro-2-methoxybenzohydroxamic acid derivatives and use as herbicidal agents |
US6312679B1 (en) | 1986-08-18 | 2001-11-06 | The Dow Chemical Company | Dense star polymer conjugates as dyes |
US5004863B2 (en) | 1986-12-03 | 2000-10-17 | Agracetus | Genetic engineering of cotton plants and lines |
US5015580A (en) | 1987-07-29 | 1991-05-14 | Agracetus | Particle-mediated transformation of soybean plants and lines |
EP0270496B1 (de) | 1986-12-05 | 1993-03-17 | Ciba-Geigy Ag | Verbessertes Verfahren zur Transformation von pflanzlichen Protoplasten |
CA1293974C (en) | 1986-12-29 | 1992-01-07 | Richard G. Hebbourn | Preparation of alkanolamine salts of carboxylic acid herbicides |
US5668085A (en) | 1987-04-29 | 1997-09-16 | Monsanto Company | Glyphosate formulations comprising alkoxylated amine surfactants |
ES2058337T5 (es) | 1987-04-29 | 2005-10-01 | Monsanto Europe S.A. | Formulaciones mejoradas de glifosato. |
DE3719264A1 (de) | 1987-06-10 | 1988-12-29 | Hoechst Ag | Fluessige pestizide mischformulierungen |
US5250500A (en) | 1988-02-08 | 1993-10-05 | Floratine Products Group | Herbicidal compositions containing tetrapotassium pyrophosphate as spray adjuvant |
US5416011A (en) | 1988-07-22 | 1995-05-16 | Monsanto Company | Method for soybean transformation and regeneration |
NZ230497A (en) | 1988-09-02 | 1992-05-26 | Du Pont | Layered, granular water-soluble or water-dispersible pesticide |
US5035738A (en) | 1988-12-23 | 1991-07-30 | Sandoz Ltd. | Aminopropylmorpholine salts, compositions and uses thereof |
NZ231897A (en) | 1988-12-30 | 1992-09-25 | Monsanto Co | Dry water-soluble granular composition comprising glyphosate and a liquid surfactant |
US5550318A (en) | 1990-04-17 | 1996-08-27 | Dekalb Genetics Corporation | Methods and compositions for the production of stably transformed, fertile monocot plants and cells thereof |
US7705215B1 (en) | 1990-04-17 | 2010-04-27 | Dekalb Genetics Corporation | Methods and compositions for the production of stably transformed, fertile monocot plants and cells thereof |
US5484956A (en) | 1990-01-22 | 1996-01-16 | Dekalb Genetics Corporation | Fertile transgenic Zea mays plant comprising heterologous DNA encoding Bacillus thuringiensis endotoxin |
CA2074355C (en) | 1990-01-22 | 2008-10-28 | Ronald C. Lundquist | Method of producing fertile transgenic corn plants |
US5834006A (en) | 1990-04-05 | 1998-11-10 | Dow Agrosciences Llc | Latex-based agricultural compositions |
US5703015A (en) | 1990-08-09 | 1997-12-30 | Monsanto Company | Pesticidal compositions of polyoxyalkylene alkylamine surfactants having reduced eye irritation |
US6403865B1 (en) | 1990-08-24 | 2002-06-11 | Syngenta Investment Corp. | Method of producing transgenic maize using direct transformation of commercially important genotypes |
DE4030687A1 (de) | 1990-09-28 | 1991-05-16 | Kast Walter Klaus Dr Sc Agr | Mittel zur selektiven abtoetung unerwuenschter pflanzen (herbizid) im wein- und obstbau unter verwendung von essigsaeure natuerlichen oder synthetischen ursprungs |
US5384253A (en) | 1990-12-28 | 1995-01-24 | Dekalb Genetics Corporation | Genetic transformation of maize cells by electroporation of cells pretreated with pectin degrading enzymes |
CA2100339A1 (en) | 1991-01-24 | 1992-07-25 | Erhard John Prill | Glyphosate formulations |
FR2675014B1 (fr) | 1991-04-09 | 1993-06-25 | Rhone Poulenc Chimie | Compositions aqueuses de matieres actives phytosanitaires comportant des sucroglycerides. |
US5883046A (en) | 1991-06-05 | 1999-03-16 | Sandoz Ltd. | Microencapsulated agricultural chemicals |
US5733848A (en) | 1991-06-05 | 1998-03-31 | Sandoz Ltd. | Process for making microparticulate agricultural chemicals |
US5221319A (en) | 1991-08-16 | 1993-06-22 | Pbi-Gordon Corporation | Dry, water-soluble, substituted phenoxy and/or benzoic acid herbicidal compositions and method of preparing same |
US5518908A (en) | 1991-09-23 | 1996-05-21 | Monsanto Company | Method of controlling insects |
US5266553A (en) | 1991-10-21 | 1993-11-30 | Riverdale Chemical Company | Method of manufacturing a dry water-soluble herbicidal salt composition |
US5229354A (en) | 1992-02-28 | 1993-07-20 | Isp Investments Inc. | Leaching inhibition of crop treating chemicals with nitrogen containing polymers |
US5231070A (en) | 1992-02-28 | 1993-07-27 | Isp Investments Inc. | Leaching inhibition of crop treating chemicals with lactam containing polymers |
US5229355A (en) | 1992-02-28 | 1993-07-20 | Isp Investments Inc. | Leaching inhibition of crop treating chemicals with polymers |
US5283228A (en) | 1992-07-27 | 1994-02-01 | Isp Investments, Inc. | Leaching inhibition of crop treating chemicals with amino containing polymers |
GB2267825B (en) | 1992-05-26 | 1995-08-30 | Dowelanco | Herbicidal aqueous-based microemulsion compositions |
ATE398679T1 (de) | 1992-07-07 | 2008-07-15 | Japan Tobacco Inc | Verfahren zur transformation einer monokotyledon pflanze |
US5317003A (en) | 1992-07-16 | 1994-05-31 | Monsanto Company | Herbicidal compositions comprising glyphosate salts and alkoxylated quaternary amine surfactants |
JP3345930B2 (ja) | 1993-01-06 | 2002-11-18 | 日産自動車株式会社 | アクティブコントロール装置 |
US5565409A (en) | 1993-04-02 | 1996-10-15 | Monsanto Company | Liquid concentrated herbicidal microemulsion compositions comprising glyphosate and either oxyfluorfen or acifluorfen |
US5374603A (en) | 1993-04-23 | 1994-12-20 | Dowelanco | Agricultural formulations comprising fluroxypyr esters which are liquid at 25° C. |
AU691228B2 (en) | 1993-12-17 | 1998-05-14 | Monsanto Technology Llc | Surfactants providing enhanced efficacy and/or rainfastness to pesticide formulations |
US5631152A (en) | 1994-10-26 | 1997-05-20 | Monsanto Company | Rapid and efficient regeneration of transgenic plants |
DE4444708A1 (de) | 1994-12-15 | 1996-06-20 | Basf Ag | Verwendung von Herbiziden vom Auxin-Typ zur Behandlung von transgenen Kulturpflanzen |
US5643853A (en) | 1995-02-28 | 1997-07-01 | Purdue Research Foundation | Thiol activation of cytotoxic and auxin-herbicidal agents and root formation stimulation |
US5965487A (en) | 1995-03-15 | 1999-10-12 | Dow Agrosciences Llc | Mixed herbicidal compositions |
US5698210A (en) | 1995-03-17 | 1997-12-16 | Lee County Mosquito Control District | Controlled delivery compositions and processes for treating organisms in a column of water or on land |
US5750468A (en) | 1995-04-10 | 1998-05-12 | Monsanto Company | Glyphosate formulations containing etheramine surfactants |
AU691425B2 (en) | 1995-04-10 | 1998-05-14 | Monsanto Technology Llc | Glyphosate formulations containing etheramine surfactants |
CA2235146C (en) | 1995-10-25 | 2004-12-14 | E.I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
AR004705A1 (es) | 1995-11-07 | 1999-03-10 | Sabba Da Silva Lima Michele | Composicion agroquimica liquida, metodo para convertirla en un liquido estable y composicion adyuvante para la preparacion de la misma. |
DE19607633A1 (de) | 1996-02-29 | 1997-09-04 | Bayer Ag | Herbizide Mittel auf Basis von N-Phosphonomethyl-glycinestern |
EP0808569A1 (en) | 1996-05-24 | 1997-11-26 | Monsanto Europe S.A./N.V. | New herbicidal compositions and use thereof |
AUPO016596A0 (en) | 1996-05-30 | 1996-06-27 | Martin, Brendan | Herbaceous plant (weed) control formulation |
US6586367B2 (en) | 1996-09-05 | 2003-07-01 | Syngenta Crop Protection, Inc. | Process for the control of weeds |
DK0929222T3 (da) | 1996-10-07 | 2002-07-01 | Syngenta Ltd | Glyphosat-formuleringer |
US6245713B1 (en) | 1996-10-25 | 2001-06-12 | Monsanto Company | Plant treatment compositions having enhanced biological effectiveness |
US5981840A (en) | 1997-01-24 | 1999-11-09 | Pioneer Hi-Bred International, Inc. | Methods for agrobacterium-mediated transformation |
PL195763B1 (pl) | 1997-06-30 | 2007-10-31 | Monsanto Technology Llc | Kompozycja do kontrolowanego uwalniania zapewniająca środek grzybobójczy roślinie i sposób wytwarzania kompozycji |
WO1999004635A1 (en) | 1997-07-22 | 1999-02-04 | Monsanto Company | High-loaded ammonium glyphosate formulations |
US6133199A (en) | 1997-07-30 | 2000-10-17 | Monsanto Company | Process and compositions promoting biological effectiveness of exogenous chemical substances in plants |
US5877112A (en) | 1997-08-27 | 1999-03-02 | Helena Chemical Company | Agricultural formulation |
DE19815820A1 (de) | 1998-04-08 | 1999-10-14 | Hoechst Schering Agrevo Gmbh | Synergistische herbizide Mittel auf Basis von phosphorhaltigen Blattherbiziden, Imidazolinonen und Wuchsstoffherbiziden |
DK1100326T3 (da) | 1998-07-29 | 2003-08-11 | Syngenta Ltd | Mikrokapsler med base-udløst frigivelse |
DE69905903T2 (de) | 1998-07-30 | 2003-11-06 | Syngenta Ltd | Mikrokapseln mit von säuren ausgelöste freisetzung |
DE19836737A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Maiskulturen |
DE19836700A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
EP2319315B2 (de) | 1998-08-13 | 2018-02-21 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Maiskulturen |
DE19836684A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Reiskulturen |
DE19836660A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Sojakulturen |
DE19836726A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante und resistente Rapskulturen |
GB9819693D0 (en) | 1998-09-10 | 1998-11-04 | Zeneca Ltd | Glyphosate formulation |
CA2351386C (en) | 1998-11-23 | 2008-06-03 | Monsanto Co. | Highly concentrated aqueous glyphosate compositions |
DK1438896T3 (en) | 1998-11-23 | 2015-11-16 | Monsanto Technology Llc | Compact storage and transport system for glyphosate herbicides |
DE69922996T2 (de) * | 1998-11-30 | 2005-12-22 | Flamel Technologies | Förderung der biologischen effektivität exogener chemischer substanzen in pflanzen |
JP2002534129A (ja) | 1999-01-14 | 2002-10-15 | モンサント テクノロジー エルエルシー | ダイズ形質転換方法 |
US6432878B1 (en) | 1999-01-15 | 2002-08-13 | Cognis Corporation | Adjuvant composition |
PT1023832E (pt) | 1999-01-29 | 2005-02-28 | Basf Ag | Concentrado em suspensao aquosa |
UA72761C2 (en) | 1999-04-23 | 2005-04-15 | Monsanto Technology Llc | Compositions and method of eliminating plant growth or controlling thereof |
AUPQ017699A0 (en) | 1999-05-05 | 1999-05-27 | Victorian Chemicals International Pty Ltd | Agrochemical composition |
US6774087B1 (en) | 1999-06-22 | 2004-08-10 | Fmc Corporation | Liquid herbicide composition |
US6713433B2 (en) | 1999-08-11 | 2004-03-30 | Monsanto Technology, Llc | Coformulation of an oil-soluble herbicide and a water-soluble herbicide |
US6908882B1 (en) | 1999-09-09 | 2005-06-21 | Monsanto Company | Enhanced method of killing weeds with glyphosate herbicide |
JP5433120B2 (ja) | 1999-09-30 | 2014-03-05 | モンサント テクノロジー エルエルシー | 向上した安定性を有するパッケージミックス農薬組成物 |
CN1192707C (zh) | 1999-10-26 | 2005-03-16 | 陶氏益农有限责任公司 | 除草剂的浓悬浮剂 |
CA2390564A1 (en) | 1999-11-17 | 2001-05-25 | Bayer Aktiengesellschaft | Selective herbicides based on 2,6-disubstituted pyridine derivatives |
US6939555B2 (en) | 2000-01-21 | 2005-09-06 | Helena Holding Company | Manufacture and use of an deposition aid |
MY158895A (en) | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
US6992045B2 (en) | 2000-05-19 | 2006-01-31 | Monsanto Technology Llc | Pesticide compositions containing oxalic acid |
US7135437B2 (en) | 2000-05-19 | 2006-11-14 | Monsanto Technology Llc | Stable liquid pesticide compositions |
US6300323B1 (en) | 2000-08-08 | 2001-10-09 | Ishihara Sangyo Kaisha, Ltd. | (Poly)ethereal ammonium salts of herbicides bearing acidic moieties and their use as herbicides |
US7008904B2 (en) | 2000-09-13 | 2006-03-07 | Monsanto Technology, Llc | Herbicidal compositions containing glyphosate and bipyridilium |
US6410783B1 (en) | 2000-10-19 | 2002-06-25 | Basf Corporation | Method of producing carboxylic acid salts |
US8232230B2 (en) | 2000-12-01 | 2012-07-31 | Helena Holding Company | Manufacture and use of a herbicide formulation |
US6992047B2 (en) | 2001-04-11 | 2006-01-31 | Monsanto Technology Llc | Method of microencapsulating an agricultural active having a high melting point and uses for such materials |
EP1389040B1 (en) | 2001-05-21 | 2010-05-19 | Monsanto Technology LLP | Pesticide concentrates containing etheramine surfactants |
AUPR682201A0 (en) | 2001-08-03 | 2001-08-30 | Nufarm Limited | Glyphosate composition |
EP1435778A1 (en) | 2001-09-14 | 2004-07-14 | Professor Sigge & Martin AB | Method of inhibiting plant growth or sprouting of tubers |
WO2003032729A1 (en) | 2001-09-26 | 2003-04-24 | Platte Chemical Co. | Herbicide compositions comprising imidazolinone acid |
US6767863B2 (en) | 2001-12-21 | 2004-07-27 | Dow Agrosciences Llc | High-strength low-viscosity agricultural formulations |
US6579831B1 (en) | 2002-01-30 | 2003-06-17 | Nufarms Americas Inc | Liquid herbicidal compositions and use thereof in a granular herbicide |
RU2208930C1 (ru) | 2002-02-13 | 2003-07-27 | Общество с ограниченной ответственностью "Экстерн" | Гербицидный состав для борьбы с нежелательной растительностью |
US20040138176A1 (en) | 2002-05-31 | 2004-07-15 | Cjb Industries, Inc. | Adjuvant for pesticides |
CN100531573C (zh) | 2002-08-31 | 2009-08-26 | 孟山都技术公司 | 含有二羧酸组分的干燥农药组合物的制备方法 |
CN1513326A (zh) | 2002-12-31 | 2004-07-21 | 中山市除害消毒管理站 | 一种能控制蚊虫孳生、促进植物生长的高效卫生杀虫剂 |
EP1617720A1 (en) | 2003-04-22 | 2006-01-25 | Monsanto Technology LLC | Herbicidal compositions containing glyphosate and a pyridine analog |
US20050026781A1 (en) | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
US9668471B2 (en) | 2003-05-28 | 2017-06-06 | AgQuam LLC | Manufacture and use of agricultural spray adjuvants for hard water conditions |
US20070149409A1 (en) | 2003-12-29 | 2007-06-28 | Hi-Cap Formulations Ltd. | Pesticide formulations with substituted biopolymers and organic polymers for improving residual activity, droplet size, adherence and rainfastness on leaves and reduction in soil leaching |
ATE517548T1 (de) | 2004-03-10 | 2011-08-15 | Monsanto Technology Llc | Herbizide zusammensetzungen, die n- phosphonomethylglycin und ein auxinherbizid enthalten |
CA2897475C (en) | 2004-04-30 | 2018-07-10 | Dow Agrosciences Llc | Novel herbicide resistance genes |
WO2005115144A1 (en) | 2004-05-25 | 2005-12-08 | William Stringfellow | Pesticide composition |
US20060040828A1 (en) | 2004-08-18 | 2006-02-23 | Jianhua Mao | Biologically active formulation containing polyethyleneimine and its derivatives |
ES2317295T3 (es) | 2004-08-19 | 2009-04-16 | Monsanto Technology Llc | Composicion herbicida de sal glifosato. |
MX2007003193A (es) | 2004-09-17 | 2007-05-16 | Monsanto Technology Llc | Formulaciones de glifosato con sintomas de quemado temprano. |
EP2308460A1 (de) | 2005-02-21 | 2011-04-13 | Basf Se | Wirkstoffzusammensetzung die wenigstens ein stickstoffatomhaltiges, hyperverzweigtes Polymer enthält |
US7223718B2 (en) | 2005-03-07 | 2007-05-29 | Falcon Lab Llc | Enhanced glyphosate herbicidal concentrates |
DE102005014293A1 (de) | 2005-03-24 | 2006-09-28 | Basf Ag | Verdickungsmittel auf Basis von Amingruppen enthaltenden Polymeren |
ES2651787T3 (es) | 2005-04-26 | 2018-01-29 | Bayer Intellectual Property Gmbh | Suspoemulsiones de agua en aceite |
US7431845B2 (en) | 2005-06-23 | 2008-10-07 | Nalco Company | Method of clarifying oily waste water |
US8232265B2 (en) | 2005-10-07 | 2012-07-31 | Board Of Trustees Of The University Of Alabama | Multi-functional ionic liquid compositions for overcoming polymorphism and imparting improved properties for active pharmaceutical, biological, nutritional, and energetic ingredients |
US8883689B2 (en) | 2005-12-06 | 2014-11-11 | Bayer Cropscience Lp | Stabilized herbicidal compositions |
US20070184980A1 (en) | 2006-01-25 | 2007-08-09 | Helena Holding Company | Manufacture and use of herbicide chlorinated phenoxy formulation |
US7446352B2 (en) * | 2006-03-09 | 2008-11-04 | Tela Innovations, Inc. | Dynamic array architecture |
JP5122841B2 (ja) | 2006-03-24 | 2013-01-16 | 石原産業株式会社 | 除草組成物 |
CA2645263A1 (en) | 2006-03-24 | 2007-10-04 | Basf Se | Agrochemical formulations |
US7855326B2 (en) | 2006-06-06 | 2010-12-21 | Monsanto Technology Llc | Methods for weed control using plants having dicamba-degrading enzymatic activity |
CN101534637A (zh) | 2006-09-06 | 2009-09-16 | 先正达参股股份有限公司 | 固体稳定乳液制剂 |
GB0703394D0 (en) | 2007-02-22 | 2007-03-28 | Ciba Sc Holding Ag | Process for Preparing and Applying Pesticide or Herbicide Formulation |
CN101621925A (zh) | 2007-02-26 | 2010-01-06 | 陶氏益农公司 | 衍生自羧酸除草剂和一些三烷基胺或杂芳基胺的离子液体 |
MX2009008934A (es) | 2007-02-26 | 2009-08-28 | Dow Agrosciences Llc | Proceso para la preparacion de algunas sulfiliminas sustituidas. |
RU2366176C2 (ru) | 2007-03-13 | 2009-09-10 | Закрытое акционерное общество промышленная группа "Алсико" | Гербицидный состав и способ борьбы с сорными растениями |
EP2308309B1 (en) | 2007-06-29 | 2013-07-31 | Dow AgroSciences LLC | Synergistic herbicidal composition containing a substituted phenoxy alkanoic acid derivative and a glyphosate derivative |
MX2010002340A (es) | 2007-08-30 | 2010-05-14 | Dow Agrosciences Llc | Formulacion en emulsion estable que dificulta la interaccion a traves de la interfase agua-aceite. |
CN101932236A (zh) | 2007-11-07 | 2010-12-29 | 罗地亚管理公司 | 包含氨基磷酸盐或氨基膦酸盐和粘度降低剂的除草组合物 |
US7695541B1 (en) | 2008-03-24 | 2010-04-13 | Frizzell Raymond B | Non-acidic, high calcium load aqueous fertilizer |
PL2337452T3 (pl) | 2008-07-03 | 2015-05-29 | Monsanto Technology Llc | Połączenia derywatyzowanych sacharydowych środków powierzchniowo czynnych i środków powierzchniowo czynnych stanowiących tlenek eteroaminy jako adiuwanty do herbicydów |
AR075466A1 (es) | 2008-10-22 | 2011-04-06 | Basf Se | Uso de herbicidas tipo auxina en plantas cultivadas |
AU2010202620B2 (en) | 2008-12-23 | 2013-10-31 | Nufarm Australia Limited | Dicamba herbicide composition |
PL2381771T3 (pl) | 2008-12-23 | 2014-08-29 | Nufarm Australia Ltd | Kompozycja auksynowych herbicydów |
RU2384064C1 (ru) | 2008-12-29 | 2010-03-20 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Гербицидное средство |
RU2395203C1 (ru) | 2009-01-21 | 2010-07-27 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Гербицидная композиция |
AU2010221301B2 (en) | 2009-03-06 | 2015-03-19 | Jones Iii, Charles A. | Compatibilized electrolyte formulations |
PT2421372E (pt) | 2009-04-22 | 2013-08-22 | Dow Agrosciences Llc | Composições de sais de glifosato e de 2,4-d, herbicidas de alta potência |
WO2010147966A1 (en) | 2009-06-15 | 2010-12-23 | Accuform Technologies, Llc | Reduced vaporization compositions and methods |
US20110019652A1 (en) | 2009-06-16 | 2011-01-27 | Powerwave Cognition, Inc. | MOBILE SPECTRUM SHARING WITH INTEGRATED WiFi |
WO2011019652A2 (en) * | 2009-08-10 | 2011-02-17 | Monsanto Technology Llc | Low volatility auxin herbicide formulations |
CN107148970B (zh) | 2009-09-02 | 2022-01-11 | 阿克苏诺贝尔化学品国际有限公司 | 用于农业的含氮表面活性剂 |
PL2638803T3 (pl) | 2009-09-30 | 2017-08-31 | Basf Corporation | Nisko lotne sole aminowe pestycydów anionowych |
RU2408188C1 (ru) | 2009-11-17 | 2011-01-10 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Гербицидное средство |
WO2011082162A1 (en) | 2009-12-29 | 2011-07-07 | Syngenta Participations Ag | Pesticidal composition |
WO2011140020A2 (en) | 2010-05-04 | 2011-11-10 | Dow Agrosciences Llc | Synergistic herbicidal composition containing a dicamba derivative and a glyphosate derivative |
ES2621972T3 (es) * | 2010-10-01 | 2017-07-05 | Nufarm Australia Limited | Método para la preparación de un concentrado acuoso de glifosato |
WO2012092078A1 (en) * | 2010-12-28 | 2012-07-05 | Castle Surgical, Inc. | Sliding overhead clip and associated methods |
GB201101743D0 (en) | 2011-02-01 | 2011-03-16 | Syngenta Ltd | Herbicidal compositions |
EP2713717A1 (en) | 2011-06-01 | 2014-04-09 | Basf Se | Method of preparing an aqueous tank mix comprising a base |
US10334849B2 (en) | 2011-10-26 | 2019-07-02 | Monsanto Technology Llc | Salts of carboxylic acid herbicides |
WO2013184622A2 (en) * | 2012-06-04 | 2013-12-12 | Monsanto Technology Llc | Aqueous concentrated herbicidal compositions containing glyphosate salts and dicamba salts |
CA2901680C (en) * | 2013-02-27 | 2021-09-07 | Monsanto Technology Llc | Glyphosate composition for dicamba tank mixtures with improved volatility |
-
2014
- 2014-02-27 CA CA2901680A patent/CA2901680C/en active Active
- 2014-02-27 ES ES14756379.5T patent/ES2694509T3/es active Active
- 2014-02-27 AU AU2014223496A patent/AU2014223496B2/en active Active
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- 2014-02-27 AR ARP140100620A patent/AR094909A1/es unknown
- 2014-02-27 EP EP14756379.5A patent/EP2961276B1/en active Active
- 2014-02-27 CA CA3123573A patent/CA3123573C/en active Active
- 2014-02-27 CA CA3123572A patent/CA3123572A1/en not_active Abandoned
- 2014-02-27 CN CN201480010587.2A patent/CN105072912A/zh active Pending
- 2014-02-27 MX MX2015011054A patent/MX2015011054A/es unknown
- 2014-02-27 BR BR112015020639-5A patent/BR112015020639B1/pt active IP Right Grant
- 2014-02-27 TR TR2018/15726T patent/TR201815726T4/tr unknown
- 2014-02-27 CN CN201910799457.6A patent/CN110495471A/zh active Pending
- 2014-02-27 PL PL14756379T patent/PL2961276T3/pl unknown
- 2014-02-27 DK DK14756379.5T patent/DK2961276T3/en active
- 2014-02-27 HU HUE14756379A patent/HUE040466T2/hu unknown
- 2014-02-27 UY UY0001035352A patent/UY35352A/es active IP Right Grant
- 2014-02-27 WO PCT/US2014/018829 patent/WO2014134235A1/en active Application Filing
-
2016
- 2016-07-01 HK HK16107668.8A patent/HK1219621A1/zh not_active IP Right Cessation
-
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- 2019-05-13 US US16/410,731 patent/US11399544B2/en active Active
- 2019-10-28 AR ARP190103111A patent/AR116874A2/es active IP Right Grant
-
2022
- 2022-04-22 US US17/726,611 patent/US20220240514A1/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060270556A1 (en) * | 2005-05-24 | 2006-11-30 | Wright Daniel R | Herbicide compatibility improvement |
US20100113274A1 (en) * | 2008-09-29 | 2010-05-06 | Monsanto Technology Llc | Glyphosate formulations containing amidoalkylamine surfactants |
US20100331182A1 (en) * | 2009-06-25 | 2010-12-30 | Dow Agrosciences Llc | Herbicidal concentrate compositions containing glyphosate and dicamba salts |
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AR116874A2 (es) | 2021-06-23 |
BR112015020639B1 (pt) | 2021-02-09 |
DK2961276T3 (en) | 2018-11-19 |
CN105072912A (zh) | 2015-11-18 |
CA2901680C (en) | 2021-09-07 |
CA3123573C (en) | 2023-10-24 |
CA3123573A1 (en) | 2014-09-04 |
CN110495471A (zh) | 2019-11-26 |
PL2961276T3 (pl) | 2019-01-31 |
ES2694509T3 (es) | 2018-12-21 |
HUE040466T2 (hu) | 2019-03-28 |
US20220240514A1 (en) | 2022-08-04 |
CA2901680A1 (en) | 2014-09-04 |
US20140249026A1 (en) | 2014-09-04 |
AR094909A1 (es) | 2015-09-09 |
UY35352A (es) | 2014-09-30 |
EP2961276B1 (en) | 2018-08-08 |
BR112015020639A2 (pt) | 2017-07-18 |
US20190335754A1 (en) | 2019-11-07 |
US10285404B2 (en) | 2019-05-14 |
TR201815726T4 (tr) | 2018-11-21 |
MX2015011054A (es) | 2015-10-22 |
AU2014223496A1 (en) | 2015-09-03 |
WO2014134235A1 (en) | 2014-09-04 |
CA3123572A1 (en) | 2014-09-04 |
HK1219621A1 (zh) | 2017-04-13 |
EP2961276A4 (en) | 2016-07-13 |
US11399544B2 (en) | 2022-08-02 |
EP2961276A1 (en) | 2016-01-06 |
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